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因使用萘普生继发严重白细胞破碎性血管炎并需截肢:一例报告

Severe leukocytoclastic vasculitis secondary to the use of a naproxen and requiring amputation: a case report.

作者信息

Brown Keri, Martin Jeanine, Zito Susan

机构信息

HCA Largo Medical Center, Indian Rocks Road, Largo, Florida, 33774, USA.

出版信息

J Med Case Rep. 2010 Jul 1;4:204. doi: 10.1186/1752-1947-4-204.

Abstract

INTRODUCTION

Leukocytoclastic vasculitis (also known as hypersensitivity vasculitis and cutaneous necrotizing vasculitis) can present with various manifestations, which often delays the diagnosis and treatment. In order to show the importance of the early recognition of leukocytoclastic vasculitis, we present a case which occurred secondary to the use of a common pharmaceutical, naproxen. We were unable to find a case of leukocytoclastic vasculitis secondary to naproxen in the literature.

CASE PRESENTATION

We present the case of a 33-year-old African American woman with below the knee and bilateral digital gangrene from hypersensitivity vasculitis secondary to the non-steroidal anti-inflammatory medication naproxen.

CONCLUSION

This is an original case report focusing on the rheumatologic management of leukocytoclastic vasculitis. However, other specialties, such as internal medicine, dermatology, infectious disease, general surgery and pathology, can gain valuable information by reviewing this case report. Reporting a case of leukocytoclastic vasculitis secondary to treatment with naproxen will advance our understanding of this disease etiology by adding yet another non-steroidal anti-inflammatory drug to the list of potential causes of leukocytoclastic vasculitis.

摘要

引言

白细胞破碎性血管炎(也称为超敏性血管炎和皮肤坏死性血管炎)可表现出多种症状,这常常会延误诊断和治疗。为了说明早期识别白细胞破碎性血管炎的重要性,我们报告一例继发于常用药物萘普生使用的病例。我们在文献中未能找到继发于萘普生的白细胞破碎性血管炎病例。

病例介绍

我们报告一例33岁非裔美国女性病例,因非甾体类抗炎药萘普生继发超敏性血管炎,出现膝下及双侧手指坏疽。

结论

这是一篇聚焦白细胞破碎性血管炎风湿病学管理的原始病例报告。然而,其他专业,如内科、皮肤科、传染病科、普通外科和病理学,通过查阅本病例报告也可获得有价值的信息。报告一例继发于萘普生治疗的白细胞破碎性血管炎病例,通过在白细胞破碎性血管炎潜在病因列表中增加另一种非甾体类抗炎药,将增进我们对该疾病病因的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31d7/2906497/169e70dc64d5/1752-1947-4-204-1.jpg

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